Experienced Clinical Research Associate, Multi-Sponsor, France

External Job Description

**Job Overview**

Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

**Essential Functions**

+ Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
+ Work with experienced clinical staff.
+ Perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
+ Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
+ Ensure the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regul...